Tracking the Evolution of Ionomer Film and Catalyst Material to Unravel PEMFC Performance Degradation

离聚物 降级(电信) 材料科学 催化作用 质子交换膜燃料电池 化学工程 复合材料 燃料电池 化学 工程类 聚合物 电气工程 有机化学 共聚物
作者
Florian Chabot,Porcar Lionel,Laure Guétaz,Sébastien Rosini,Arnaud Morin
出处
期刊:Journal of The Electrochemical Society [Institute of Physics]
卷期号:171 (12): 124506-124506
标识
DOI:10.1149/1945-7111/ada111
摘要

Several characterization techniques were performed on a proton exchange membrane fuel cell (PEMFC) to relate the performance degradation induced by the membrane-targeted accelerated stress test (AST) to the evolution of electrochemical and physical properties of the electrode. This works investigated the ionomer structure and the proton transport properties. Electron microscopy and small angle neutron scattering analysis provided access to the electrode’s nanoscale structure, the distribution of the platinum particle size, the structure of the 2–3 nm thick ionomer film, as well as the location of the water uptake by the electrode. A newly-developed technique using proton desorption under diluted O 2 allows to distinguish effectively used active sites for oxygen reduction reaction. Proton transport and dioxygen diffusivity properties were measured using impedance spectroscopy and limiting current technique respectively. The Membrane-AST leads to an increase in the water uptake of the electrode due to a modification of the global structure of the electrode, a reduced platinum surface area, and corrosion of carbon particles. However, it does not alter the ionomer structure. The decrease in performance is partially attributed to the increase in proton resistivity, but mainly due to the limitation of dioxygen transport fostered by the electrode structure modifications.
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